ENST00000559133.6:c.*331C>A
|
ENSP00000453958.2:n.*331C>A
|
|
ENST00000674301.2:c.*1036C>A
|
ENSP00000501333.2:n.*1036C>A
|
|
ENST00000682170.1:n.1704C>A
|
|
|
ENST00000682767.1:n.820C>A
|
|
|
ENST00000316623.10:c.7523C>A
MANE Select
|
ENSP00000325527.5:p.Thr2508Lys
|
|
ENST00000674301.1:c.2689C>A
|
ENSP00000501333.1:n.2689C>A
|
|
ENST00000316623.9:c.7523C>A
|
ENSP00000325527.5:p.Thr2508Lys
|
|
ENST00000559133.5:c.2892C>A
|
|
|
NM_000138.4:c.7523C>A , LRG_778t1:c.7523C>A
|
NP_000129.3:p.Thr2508Lys
|
|
NM_000138.5:c.7523C>A
MANE Select
|
NP_000129.3:p.Thr2508Lys
|
|